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NMDAR1 (D65B7) Rabbit mAb

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  • 询价
  • Cell Signaling Technology已认证
  • USA
  • 2025年11月16日
  • W, IP
  • H,M,R
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    • 详细信息
    • 询价记录
    • 文献和实验
    • 技术资料
    • 抗体英文名

      NMDAR1 (D65B7) Rabbit mAb

    • 抗原

      synthetic peptide corresponding to residues surrounding Pro660 of human NMDAR1

    • 应用范围

      W, IP

    • 保质期

      详见说明书

    • 适应物种

      H,M,R

    • 库存

      大量

    • 级别

      详见MSDS文件

    • 供应商

      CST

    • 是否单克隆

      1

    • 保存条件

      -20°c

    • 规格

      100 ul (10 western blots)/carrier free & custom formulation / quantity

    规格:产品价格:¥请询价
    规格:100 ul (10 western blots)产品价格:¥请询价
    规格:carrier free & custom formulation / quantity产品价格:¥请询价

    pathway more info application references datasheet PDF MSDS PDF protocols

    Applications Key:  W=Western Blotting  IP=Immunoprecipitation
    Reactivity Key:  H=Human  M=Mouse  R=Rat
    Species cross-reactivity is determined by western blot. Species enclosed in parentheses are predicted to react based on 100% sequence homology.

    Applications Reactivity Sensitivity MW (kDa) Isotype
    W IP H M R Endogenous 120 Rabbit IgG
    Protocols
    Specificity / Sensitivity

    NMDAR1 (D65B7) Rabbit mAb detects endogenous levels of total NMDAR1 protein.

    Source / Purification

    Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to residues surrounding Pro660 of human NMDAR1.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from rat and mouse brain using NMDAR1 (D65B7) Rabbit mAb.

    Background

    N-methyl-D-aspartate receptor (NMDAR) forms a heterodimer of at least one NR1 and one NR2A-D subunit. Multiple receptor isoforms with distinct brain distributions and functional properties arise by selective splicing of the NR1 transcripts and differential expression of the NR2 subunits. NR1 subunits bind the co-agonist glycine and NR2 subunits bind the neurotransmitter glutamate. Activation of the NMDA receptor or opening of the ion channel allows flow of Na+ and Ca2+ ions into the cell, and K+ out of the cell (1). Each subunit has a cytoplasmic domain that can be directly modified by the protein kinase/phosphatase (2). PKC can phosphorylate the NR1 subunit (NMDAR1) of the receptor at Ser890/Ser896, and PKA can phosphorylate NR1 at Ser897 (3). The phosphorylation of NR1 by PKC decreases its affinity for calmodulin, thus preventing the inhibitory effect of calmodulin on NMDAR (4). The phosphorylation of NR1 by PKA probably counteracts the inhibitory effect of calcineurin on the receptor (5). NMDAR mediates long-term potentiation and slow postsynaptic excitation, which play central roles in learning, neurodevelopment, and neuroplasticity (6).

    1. Liu, X.B. et al. (2004) J. Neurosci. 24, 8885-8895.
    2. Westphal, R.S. et al. (1999) Science 285, 93-96.
    3. Tingley, W.G. et al. (1997) J. Biol. Chem. 272, 5157-5166.
    4. Hisatsune, C. et al. (1997) J. Biol. Chem. 272, 20805-20810.
    5. Raman, I.M. et al. (1996) Neuron 16, 415-421.
    6. Makhinson, M. et al. (1999) J. Neurosci. 19, 2500-2510.
    Application References

    Have you published research involving the use of our products? If so we'd love to hear about it. Please let us know !

    Companion Products

    For Research Use Only. Not For Use In Diagnostic Procedures.

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